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The Pathology of Incipient Polymicrogyria
Brain and Development, 2017To characterise the early tissue changes of post encephaloclastic polymicrogyria in the human fetus.We identified and reviewed the clinical histories and autopsy pathology of post ischemic fetal cerebral cortical injury at less than 30weeks gestational age (GA). The histology of local cortical abnormalities was examined with neuronal, glial, microglial
Phedias Diamandis +2 more
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Diverse Genetic Causes of Polymicrogyria With Epilepsy [PDF]
Epilepsia, 2021 OBJECTIVE: We sought to identify novel genes and to establish the contribution of known genes in a large cohort of patients with nonsyndromic sporadic polymicrogyria and epilepsy.
Kristen Park +2 more
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Bilateral Symmetrical Frontoparietal Polymicrogyria
European Journal of Paediatric Neurology, 2002A patient with bilateral symmetrical frontoparietal polymicrogyria is reported. Severe developmental delay, mental retardation, spastic tetraplegia, and seizures were the main clinical features. Magnetic resonance imaging revealed bilateral thick cortex with irregular gyri and festoon-like grey-white matter junction in the frontoparietal areas ...
László Sztriha
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De novo mutations in GRIN1 cause extensive bilateral polymicrogyria [PDF]
Brain, 2018 Polymicrogyria is a malformation of cortical development. The aetiology of polymicrogyria remains poorly understood. Using whole-exome sequencing we found de novo heterozygous missense GRIN1 mutations in 2 of 57 parent-offspring trios with polymicrogyria.
Fabienne GIULIANO +2 more
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Polymicrogyria With Dysmorphic Basal Ganglia? Think Tubulin! [PDF]
Clinical Genetics, 2014 Dominant mutations in TUBB2B have been reported in patients with polymicrogyria. We further explore the phenotype associated with mutations in TUBB2B.
Tim Vanderhasselt +2 more
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Bilateral Frontoparietal Polymicrogyria
The Indian Journal of Pediatrics, 2014Two male siblings, aged 4.5 and 10 y respectively, of a nonconsanguinous family, presented with delayed milestones and epilepsy. The older sibling had frequent seizures since 7 y of age. Seizures were generalized-tonic-clonic and were poorly controlled on valproate, phenytoin and clobazam.
Puneet, Jain +4 more
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Management of the Child With Polymicrogyria
Journal of Neuroscience Nursing, 2009Polymicrogyria is one of several neuronal migrational defects. This disorder is derived from a malformation in cortical development characterized by many small gyri, shallow sulci, and abnormal cortical layering. The potential causes of polymicrogyria include genetic disorders, intrauterine cytomegalovirus infection, and fetal vascular supply ...
Sandra L, Turkelson, Caron, Martin
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Bilateral opercular polymicrogyria
Annals of Neurology, 1989Abstract Foix‐Chavany‐Marie syndrome (FCMS), or faciopharyngoglossomasticatory diplegia, is an uncommon syndrome that can result from vascular or developmental lesions of the anterior opercula bilaterally. We report the first pathological documentation of the developmental form of this disorder.
P S, Becker, A M, Dixon, J C, Troncoso
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